R.L. Stallings

Rare Deletions at 16p13.11 Predispose to a Diverse Spectrum of Sporadic Epilepsy Syndromes

Erin L. Heinzen, Rodney A. Radtke, Thomas Urban et al. · The American Journal of Human Genetics · 2010 · 259 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Coordinate Deletion of Chromosome 3p and 11q in Neuroblastoma Detected by Comparative Genomic Hybridization

Claire J. Breen, Anne O’Meara, Michael McDermott et al. · Cancer Genetics and Cytogenetics · 2000 · 64 citations

Life Sciences, Genetics, Molecular Genetics +10

Minimal residual disease detection in childhood acute lymphoblastic leukaemia patients at multiple time‐points reveals high levels of concordance between molecular and immunophenotypic approaches

Jacqueline Ryan, Fiona Quinn, Armelle Meunier et al. · British Journal of Haematology · 2008 · 55 citations · Full text

Medicine, Hematology, Oncology +16

Orchestrating osteogenic differentiation of mesenchymal stem cells—identification of placental growth factor as a mechanosensitive gene with a pro-osteogenic role

Ryan McCoy, Amro Widaa, Karen M. Watters et al. · Stem Cells · 2013 · 51 citations · Full text

Engineering, Bioengineering, Cell Biology +17

Fine Genetic Mapping of the Batten Disease Locus (CLN3) by Haplotype Analysis and Demonstration of Allelic Association with Chromosome 16p Microsatellite Loci

Hannah M. Mitchison, Andrew Thompson, John C. Mulley et al. · Genomics · 1993 · 48 citations

Life Sciences, Genetics, Molecular Genetics +17